Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C1836479
Disease: Saccadic smooth pursuit
Saccadic smooth pursuit 		22 0 7 0.15 0 0
CUI: C0271390
Disease: Nystagmus, End-Position
Nystagmus, End-Position 		26 0 6 0.12 0 0
CUI: C0752122
Disease: Spinocerebellar Ataxia Type 4
Spinocerebellar Ataxia Type 4 		36 0 7 0.11 0 0
CUI: C1835265
Disease: Lymphedema, microcephaly and chorioretinopathy syndrome
Lymphedema, microcephaly and chorioretinopathy syndrome 		7 0 4 0.11 0 0
CUI: C0750937
Disease: Ataxia, Appendicular
Ataxia, Appendicular 		86 0 12 0.11 0 0
CUI: C0234979
Disease: Dysdiadochokinesis
Dysdiadochokinesis 		49 0 8 0.11 0 0
CUI: C1853394
Disease: Gaze-evoked horizontal nystagmus
Gaze-evoked horizontal nystagmus 		10 0 4 0.11 0 0
CUI: C0234162
Disease: Cerebellar Dysmetria
Cerebellar Dysmetria 		127 0 15 0.10 0 0
CUI: C0239882
Disease: Head tremor
Head tremor 		21 0 5 0.10 0 0
CUI: C1853761
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1 		21 0 5 0.10 0 0
CUI: C0087012
Disease: Ataxia, Spinocerebellar
Ataxia, Spinocerebellar 		156 0 17 9.9E-02 0 0
CUI: C0278184
Disease: Scanning speech
Scanning speech 		13 0 4 9.8E-02 0 0
CUI: C1837458
Disease: Impaired smooth pursuit
Impaired smooth pursuit 		25 0 5 9.6E-02 0 0
CUI: C0752123
Disease: Spinocerebellar Ataxia Type 5
Spinocerebellar Ataxia Type 5 		48 0 7 9.6E-02 0 0
CUI: C4024900
Disease: Atrophy/Degeneration affecting the brainstem
Atrophy/Degeneration affecting the brainstem 		27 0 5 9.3E-02 0 0
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia 		172 0 17 9.1E-02 0 0
CUI: C0752124
Disease: Spinocerebellar Ataxia Type 6 (disorder)
Spinocerebellar Ataxia Type 6 (disorder) 		64 0 8 9.1E-02 0 0
CUI: C0752125
Disease: Spinocerebellar Ataxia Type 7
Spinocerebellar Ataxia Type 7 		78 0 9 8.9E-02 0 0
CUI: C1836392
Disease: Dysmetric saccades
Dysmetric saccades 		18 0 4 8.7E-02 0 0
CUI: C4087347
Disease: Autosomal dominant cerebellar ataxia
Autosomal dominant cerebellar ataxia 		31 0 5 8.6E-02 0 0
CUI: C0393525
Disease: Progressive cerebellar ataxia
Progressive cerebellar ataxia 		136 0 13 8.4E-02 0 0
CUI: C0020580
Disease: Hypesthesia
Hypesthesia 		33 0 5 8.3E-02 0 0
CUI: C0431370
Disease: Atrophy of corpus callosum
Atrophy of corpus callosum 		21 2 4 8.2E-02 1 0.14
CUI: C1843885
Disease: Progressive gait ataxia
Progressive gait ataxia 		21 0 4 8.2E-02 0 0
CUI: C1867138
Disease: Upper limb postural tremor
Upper limb postural tremor 		8 0 3 8.1E-02 0 0